Canonical Allele Identifier: PA2573221034
Gene: C9 HGNC NCBI
ClinVar RCV:
RCV002050001
ClinVar Variation:
1346020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001728.1:p.Val372Phe
CA359554886
NM_001737.5:c.1114G>T